Merola, Joseph S.Husebo, Trang Le2018-03-052018-03-052014-04-011600-5368http://hdl.handle.net/10919/82441The title compound, [Ir2H2O(C3H9P)6](BF4)2·2H2O, was isolated from the reaction between [Ir(COD)(PMe3)3]BF4 and H2 in water (COD is cyclo-octa-1,5-diene). The asymmetric unit consists of one Ir(III) atom bonded to three PMe3 groups, one hydride ligand and half an oxide ligand, in addition to a BF4 (-) counter-ion and one water molecule of hydration. The single oxide ligand bridging two Ir(III) atoms is disordered across an inversion center with each O atom having a 50% site occupancy. Each Ir(III) atom has three PMe3 groups occupying facial positions, with the half-occupancy O atoms, a hydride ligand and an Ir-Ir bond completing the coordination sphere. The Ir-Ir distance is 2.8614 (12) Å, comparable to other iridium(III) metal-metal bonds. Two water mol-ecules hydrogen bond to two BF4 (-) anions in the unit cell.m122 - m123 page(s)application/pdfCreative Commons Attribution 4.0 Internationalμ-Oxido-bis-[hydridotris(tri-methyl-phosphane-κP)iridium(III)](Ir-Ir) bis-(tetra-fluorido-borate) dihydrate.Article - RefereedActa Crystallogr Sect E Struct Rep Onlinehttps://doi.org/10.1107/S160053681400453X70Pt 44Merola, J [0000-0002-1743-1777]